chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161212492161212493GA38GENICpossibly homozygous111796964
3161212796161212797CG49GENIChomozygous111796966
3161213439161213440TC24GENIChomozygous111796968
3161214452161214453CT31GENIChomozygous111796970
3161219354161219355TG35GENIChomozygous111796972
3161219396161219397TG34GENICpossibly homozygous111796974
3161221084161221085TC44GENIChomozygous111796976
3161223070161223071AC51GENIChomozygous119652595
3161223071161223072GA51GENIChomozygous112045570
3161226752161226753TC43GENIChomozygous111796980
3161231555161231556CT31GENIChomozygous111796982
3161232624161232625AT21GENIChomozygous111796984
3161233444161233445GA44GENIChomozygous111796986